Cargando…
Hnf1b renal expression directed by a distal enhancer responsive to Pax8
Xenopus provides a simple and efficient model system to study nephrogenesis and explore the mechanisms causing renal developmental defects in human. Hnf1b (hepatocyte nuclear factor 1 homeobox b), a gene whose mutations are the most commonly identified genetic cause of developmental kidney disease,...
Autores principales: | Goea, L., Buisson, I., Bello, V., Eschstruth, A., Paces-Fessy, M., Le Bouffant, R., Chesneau, A., Cereghini, S., Riou, J. F., Umbhauer, M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9675860/ https://www.ncbi.nlm.nih.gov/pubmed/36402859 http://dx.doi.org/10.1038/s41598-022-21171-x |
Ejemplares similares
-
Hnf1b haploinsufficiency differentially affects developmental target genes in a new renal cysts and diabetes mouse model
por: Niborski, Leticia L., et al.
Publicado: (2021) -
Urinary proteome signature of Renal Cysts and Diabetes syndrome in children
por: Ricci, Pierbruno, et al.
Publicado: (2019) -
The nephrogenic potential of the transcription factors osr1, osr2, hnf1b, lhx1 and pax8 assessed in Xenopus animal caps
por: Drews, Christiane, et al.
Publicado: (2011) -
The renal lineage factor PAX8 controls oncogenic signalling in kidney cancer
por: Patel, Saroor A., et al.
Publicado: (2022) -
UnPAXing the Divergent Roles of PAX2 and PAX8 in High-Grade Serous Ovarian Cancer
por: Hardy, Laura R., et al.
Publicado: (2018)